Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs755833826
- Species
- Homo sapiens
- Symbol
- rs755833826
- Category
- Variant
- Variant type
- SNP
- Overlaps
- STT3B
- Location
- 3:31579833
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.31579833G>T
- HGVS.c name
- ENSEMBL:ENST00000295770.4:c.448G>T
- ENSEMBL:ENST00000423527.5:n.475G>T
- HGVS.p name
- :p.Ala4Ser
- ENSP00000295770:p.Ala150Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:31532638...31638548 (105.91 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction